A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16971116



Internal ID48084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:140454654..140543103hg38UCSC Ensembl
chr6:140775791..140864240hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3888450
hg1988450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466048
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16971116
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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